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Deacetylanisomycin

NMR下載 COA and HPLC MSDS下載
names：
(2R,3S,4S)-2-((4-Methoxyphenyl)methyl)-3,4-pyrrolidinediol
CAS號(hào)：
27958-06-1
MDL Number：
MF(分子式)： C12H17NO3 MW(分子量)： 223.27
EINECS: Reaxys Number:
Pubchem ID: Brand:BIOFOUNT

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中文別名	Deacetylanisomycin
英文別名	Deacetylanisomycin; (-)-Deacetylanisomycin; Anisomycin, deacetyl-.
CAS號(hào)	27958-06-1
Inchi	InChI=1S/C12H17NO3/c1-16-9-4-2-8(3-5-9)6-10-12(15)11(14)7-13-10/h2-5,10-15H,6-7H2,1H3/t10-,11+,12+/m1/s1
InchiKey	UMWAPBCLJQSOJX-WOPDTQHZSA-N
分子式 Formula	C12H17NO3
分子量 Molecular Weight	223.27
溶解度Solubility
性狀	Solid powder
儲(chǔ)藏條件 Storage conditions	Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).

產(chǎn)品說明	Deacetylanisomycin(CAS:27958-06-1):僅限應(yīng)用于工業(yè)或者科學(xué)研究過程中非醫(yī)療目的，不應(yīng)用于人類或動(dòng)物的臨床診斷以及治過程療，該產(chǎn)品非藥用，非食用。
Introduction	Deacetylanisomycin is the core structure of a family of dihydroxypyrrolidines produced by several species of Streptomyces. deacetylanisomycin is a potent growth regulator in plants.
Application1
Application2
Application3

警示圖
危險(xiǎn)性	Warning
危險(xiǎn)性警示
安全聲明
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[1]Kim JH, Curtis-Long MJ, Seo WD, Ryu YB, Yang MS, Park KH. Stereodivergent syntheses of anisomycin derivatives from D-tyrosine. J Org Chem. 2005 May 13;70(10):4082-7. PubMed PMID: 15876100.

[2]Ramirez RR, Gandhi CC, Muzzio IA, Matzel LD. Protein synthesis-dependent memory and neuronal enhancement in Hermissenda are contingent on parameters of training and retention. Learn Mem. 1998 Mar-Apr;4(6):462-77. PubMed PMID: 10701872.

[3] Kanbe K, Mimura Y, Tamamura T, Yatagai S, Sato Y, Takahashi A, Sato K, Naganawa H, Nakamura H, Takeuchi T, et al. AB3217-A, a novel anti-mite substance produced by a strain of Streptomyces platensis. J Antibiot (Tokyo). 1992 Apr;45(4):458-64. Erratum in: J Antibiot (Tokyo) 1992 Jun;45(6):C-2. PubMed PMID: 1592678.

[4] Ekong RM, Kirby GC, Patel G, Phillipson JD, Warhurst DC. Comparison of the in vitro activities of quassinoids with activity against Plasmodium falciparum, anisomycin and some other inhibitors of eukaryotic protein synthesis. Biochem Pharmacol. 1990 Jul 15;40(2):297-301. PubMed PMID: 2198027.

[5] Crow T, Forrester J. Inhibition of protein synthesis blocks long-term enhancement of generator potentials produced by one-trial in vivo conditioning in Hermissenda. Proc Natl Acad Sci U S A. 1990 Jun;87(12):4490-4. PubMed PMID: 2352932; PubMed Central PMCID: PMC54141.

6: Alkon DL, Bank B, Naito S, Chen C, Ram J. Inhibition of protein synthesis prolongs Ca2+-mediated reduction of K+ currents in molluscan neurons. Proc Natl Acad Sci U S A. 1987 Oct;84(19):6948-52. PubMed PMID: 3477819; PubMed Central PMCID: PMC299202.7: Eskin A, Yeung SJ, Klass MR. Requirement for protein synthesis in the regulation of a circadian rhythm by serotonin. Proc Natl Acad Sci U S A. 1984 Dec;81(23):7637-41. PubMed PMID: 6095312; PubMed Central PMCID: PMC392203.

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